|
NIV for COPD exacerbation
|
Non-invasive ventilation shortens hospital stay,
reduces the need for intubation and mortality in patients with COPD
exacerbation. Non-significant reduction in VAP.
Level of
Evidence: 1+ |
Citation/s:
Laurent Brochard, Jordi Mancebo et al: Noninvasive ventilation for acute
exacerbations of chronic obstructive pulmonary disease. NEJM 1995; 333:817-22
Lead author's name and fax: Laurent Brochard
Three-part Clinical Question: In patients with COPD exacerbations, does
the use of non-invasive ventilation reduce the incidence of ventilator
associated pneumonia?
Search Terms: NIV, VAP, COPD.
The Study: Non-blinded randomised controlled trial with
intention-to-treat.
The Study Patients: Adult patients admitted to 5 French ITUS over 15
months with known COPD, or a high probability of COPD, with an exacerbation of
dyspnoea accompanied by at least 2 of the following: RR>30, PaO2< 45mmHg, pH
Control group (N = 42; 42 analysed): Standard treatment -
oxygen to a max flow rate of 5l/min in order to achieve Sa02>90, SC heparin,
antibiotics, bronchodilators, steroids, aminophylline. Intubation was performed
on the presence of specific criteria.
Experimental group (N = 43; 43 analysed): The same medications
as above with the addition of periods of NIV for at least 6 hours a day. All
patients breathed spontaneously for at least 2 hours per day. The exact duration
and pattern of NIV was determined by the attending physician. Pressure support
was initially 20cm. Oxygen was administered to achieve SaO2>90. Intubation
criteria were similar to control.
The Evidence:
|
Outcome |
Time to
Outcome |
CER |
EER |
RRR |
ARR |
NNT |
|
Pneumonia
(not present on admission) |
|
0.167 |
0.047 |
72% |
0.120 |
NS |
|
95% Confidence
Intervals: |
∞ |
∞ |
∞ |
|
Intubation |
|
0.738 |
0.256 |
65% |
0.482 |
2 |
|
95% Confidence
Intervals: |
40% to 91% |
0.296 to
0.668 |
1 to 3 |
|
Death |
|
0.286 |
0.093 |
67% |
0.193 |
5 |
|
95% Confidence
Intervals: |
11% to 100% |
0.031 to
0.355 |
3 to 32 |
|
Non-Event
Outcomes |
Time to
outcome/s |
Control
group |
Experimental group |
P-value |
|
Hospital length of stay (days) |
|
35 |
23 |
0.02 |
|
Complications |
|
.48 |
.16 |
0.001 |
Comments:
Do the methods allow accurate testing of the hypothesis? There is no information
as to how sample size was determined. The limitation in oxygen flow in the
control group to 5l/min may have made intubation for hypoxia more likely in this
group, although hypoxia alone was not an indication for intubation.
Do the statistical tests correctly test the results to allow differentiation of
statistically significant results? Yes
Are the conclusions valid in light of the results? Probably
Did results get omitted, and why? No
Did they suggest areas for further research? No - A further study would
be required to give a more definitive answer to the question posed.
Did they make any recommendations based on the results and where they
appropriate? No
Is the study relevant to my clinical practice? Yes
What level of evidence does this
study represent? Level 1+
What
grade of recommendation can
I make on this result alone? B
What
grade of recommendation
can I make when this study is considered along with other available
evidence? N/A - single study in this patient group (with VAP as an
outcome).
Should I change my practice because of these results? Yes - the potential
for benefit is great and the potential for harm small, as long as NIV is carried
out appropriately.
Should I audit my current practice because of these results? Yes - audit
the use of NIV in COPD patients, and thei subsequent intubation rate.
Appraised by: B Miles; 20 May 2004
Email: barbara.miles.stob@northglasgow.scot.nhs.uk
Kill or Update By: May 20066
Printer Friendly
Version
© SICS EBM Group 2004
|